Аннотация:
Tandem electrophilic halogenation or nitration and aromatization of 3,6-dihydropyrazines, either as starting material or formed in situ from 2,5-dioxopiperazine, provides a simple, facile pathway to polyhalo- and nitro-pyrazines.
Тип публикации:
Статья
Язык публикации: английский
Образец цитирования:
I. L. Yudin, A. B. Sheremetev, O. P. Shitov, V. A. Tartakovsky, “Facile Synthesis of Polyhalo- and Nitro-pyrazines”, Mendeleev Commun., 5:5 (1995), 196–197
Образцы ссылок на эту страницу:
https://www.mathnet.ru/rus/mendc5096
https://www.mathnet.ru/rus/mendc/v5/i5/p196
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Igor L. Yudin, Aleksei B. Sheremetev, Boris B. Averkiev, Mikhail Yu. Antipin, “Furoxano[3,4-b]pyrazines: The first synthesis and x-ray structure”, Journal of Heterocyclic Chemistry, 42:4 (2005), 691
Richard Göschke, Stefan Stutz, Walter Heinzelmann, Jürgen Maibaum, “The Nonchiral Bislactim Diethoxy Ether as a Highly Stereo‐Inducing Synthon for Sterically Hindered, γ‐Branched α‐Amino Acids: A Practical, Large‐Scale Route to an Intermediate of the Novel Renin Inhibitor Aliskiren”, Helvetica Chimica Acta, 86:8 (2003), 2848
I. L. Yudin, S. M. Aronova, A. B. Sheremetev, B. B. Averkiev, M. Yu. Antipin, “Facile and general synthesis of pyrrolo[2,3-b]pyrazines via 2-(dicyanoylidene)-3-halopyrazines”, Mendeleev Commun., 11:4 (2001), 152–153
I. L. YUDIN, A. B. SHEREMETEV, O. P. SHITOV, V. A. TARTAKOVSKII, “ChemInform Abstract: Facile Synthesis of Polyhalo‐ and Nitropyrazines.”, ChemInform, 27:5 (1996)